ODCs

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6 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Malignant hyperthermia

Autosomal recessive centronuclear myopathy

CACNA1S	(UniProt - OMIM)		BIN1	(UniProt - OMIM)
RYR1	(UniProt - OMIM)		TTN	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RYR1	(0.63)	TTN

Citations in the biomedical literature:

Malignant hyperthermia		Autosomal recessive centronuclear myopathy
	Synonym(s): - Hyperthermia of anesthesia - Malignant hyperpyrexia - Pharmacogenetic myopathy of anesthesia		Synonym(s): - AR-CNM

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Injury, poisoning and certain other consequences of external causes -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

	External references: 6 OMIM references - 1 MeSH reference: D008305		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.